Canonical Allele Identifier: CA320486522

Gene: ERG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38447907C>A , CM000683.2:g.38447907C>A	GRCh38
NC_000021.8:g.39819830C>A , CM000683.1:g.39819830C>A	GRCh37
NC_000021.7:g.38741700C>A	NCBI36
NG_029732.1:g.218875G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288319.12:c.19-2286G>T MANE Select	ENSP00000288319.7:n.19-2286G>T
ENST00000288319.11:c.19-2286G>T	ENSP00000288319.7:n.19-2286G>T
ENST00000398897.5:c.-40-24346G>T	ENSP00000381871.1:n.-40-24346G>T
ENST00000398905.5:c.19-2286G>T	ENSP00000381877.1:n.19-2286G>T
ENST00000398907.5:c.19-2286G>T	ENSP00000381879.1:n.19-2286G>T
ENST00000398910.5:c.40-2286G>T	ENSP00000381881.1:n.40-2286G>T
ENST00000398911.5:c.40-2286G>T	ENSP00000381882.1:n.40-2286G>T
ENST00000398919.6:c.40-2286G>T	ENSP00000381891.2:n.40-2286G>T
ENST00000417133.6:c.40-2286G>T	ENSP00000414150.2:n.40-2286G>T
ENST00000429727.6:c.-78-2286G>T	ENSP00000415659.3:n.-78-2286G>T
ENST00000442448.5:c.40-2286G>T	ENSP00000394694.1:n.40-2286G>T
ENST00000453032.6:c.-40-24346G>T	ENSP00000396268.2:n.-40-24346G>T
ENST00000468474.5:n.226-2286G>T
ENST00000473107.1:n.84+1115G>T
ENST00000481609.5:n.190-2286G>T
NM_001136154.1:c.40-2286G>T	NP_001129626.1:n.40-2286G>T
NM_001136155.1:c.-40-24346G>T	NP_001129627.1:n.-40-24346G>T
NM_001243428.1:c.40-2286G>T	NP_001230357.1:n.40-2286G>T
NM_001243429.1:c.-40-24346G>T	NP_001230358.1:n.-40-24346G>T
NM_001243432.2:c.40-2286G>T	NP_001230361.1:n.40-2286G>T
NM_001291391.1:c.40-2286G>T	NP_001278320.1:n.40-2286G>T
NM_004449.4:c.40-2286G>T	NP_004440.1:n.40-2286G>T
NM_182918.3:c.19-2286G>T	NP_891548.1:n.19-2286G>T
XM_011529486.1:c.40-2286G>T	XP_011527788.1:n.40-2286G>T
XM_011529487.1:c.40-2286G>T	XP_011527789.1:n.40-2286G>T
NM_001331025.1:c.19-2286G>T	NP_001317954.1:n.19-2286G>T
NM_182918.4:c.19-2286G>T MANE Select	NP_891548.1:n.19-2286G>T
NM_001331025.2:c.19-2286G>T	NP_001317954.1:n.19-2286G>T